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Mendeleev Communications, 2012, Volume 22, Issue 1, Pages 29–31
DOI: https://doi.org/10.1016/j.mencom.2012.01.011
(Mi mendc2727)
 

This article is cited in 23 scientific papers (total in 23 papers)

1,3-Dipolar cycloadditions of nonstabilised azomethine ylides at 3-substituted coumarins: synthesis of 1-benzopyrano[3,4-c]pyrrolidines

V. S. Moshkina, V. Ya. Sosnovskikha, P. A. Slepukhinb, G.-V. Roeschenthalerc

a Department of Chemistry, Ural Federal University, Ekaterinburg, Russian Federation
b I.Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, Ekaterinburg, Russian Federation
c School of Engineering and Science, Jacobs University of Bremen, Bremen, Germany
Abstract: Reaction of 3-substituted coumarins with N-alkyl-α-amino acids and aldehydes proceeds regio- and stereoselectively to give 1-benzopyrano[3,4-c]pyrrolidines as a result of 1,3-dipolar cycloaddition of the intermediate azomethine ylides at the Δ3-bond of the coumarins.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (177.2 Kb)


Citation: V. S. Moshkin, V. Ya. Sosnovskikh, P. A. Slepukhin, G.-V. Roeschenthaler, “1,3-Dipolar cycloadditions of nonstabilised azomethine ylides at 3-substituted coumarins: synthesis of 1-benzopyrano[3,4-c]pyrrolidines”, Mendeleev Commun., 22:1 (2012), 29–31
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  • https://www.mathnet.ru/eng/mendc/v22/i1/p29
  • This publication is cited in the following 23 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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